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Conformationally defined adrenergic agents. III. The importance of compartmentation in the release of norepinephrine from rat atria by endo- and exo-2-methylaminobenzobicyclo-[2.2.2]octene, conformationally defined analogs of methamphetamine.

作者信息

Ruth J A, Grunewald G L, Rutledge C O

出版信息

J Pharmacol Exp Ther. 1978 Mar;204(3):615-24.

PMID:633067
Abstract
摘要

相似文献

1
Conformationally defined adrenergic agents. III. The importance of compartmentation in the release of norepinephrine from rat atria by endo- and exo-2-methylaminobenzobicyclo-[2.2.2]octene, conformationally defined analogs of methamphetamine.构象确定的肾上腺素能药物。III. 内消旋和外消旋2-甲基氨基苯并双环-[2.2.2]辛烯（甲基苯丙胺的构象确定类似物）在大鼠心房释放去甲肾上腺素过程中分隔作用的重要性。
J Pharmacol Exp Ther. 1978 Mar;204(3):615-24.
2
Conformationally defined adrenergic agents I: potentiation of levarterenol in rat vas deferens by endo- and exo- 2- aminobenzobicyclo[2.2.2]octenes, conformationally defined analogs of amphetamine.构象明确的肾上腺素能药物I：内型和外型2-氨基苯并双环[2.2.2]辛烯对大鼠输精管中去甲肾上腺素的增强作用，苯丙胺的构象明确类似物。
J Pharm Sci. 1976 Jun;65(6):920-3. doi: 10.1002/jps.2600650632.
3
Pronounced pharmacological differences arising from minor structural changes in conformationally defined amphetamine analogues. Comparative evaluation of endo- and exo-2-amino- and endo- and exo-2-(methylamino)benzobicyclo[2.2.1]heptene and -benzobicylco[2.2.2]octene analogues. Conformationally defined adrenergic agents. 4.构象限定的苯丙胺类似物微小结构变化引起的显著药理学差异。内型和外型-2-氨基以及内型和外型-2-(甲氨基)苯并双环[2.2.1]庚烯和-苯并双环[2.2.2]辛烯类似物的比较评价。构象限定的肾上腺素能药物。4.
J Med Chem. 1980 Jun;23(6):614-20. doi: 10.1021/jm00180a006.
4
Proceedings: The selective inhibition of 5-hydroxy-tryptamine re-uptake by Org 6582.研究进展：Org 6582对5-羟色胺再摄取的选择性抑制作用
Br J Pharmacol. 1976 Mar;56(3):367P-368P.
5
Efffect of exo- and endo-2-aminobenzonorbornene on the acceleration of efflux of norepinephrine from isolated perfused rabbit atria.
Res Commun Chem Pathol Pharmacol. 1978 Jul;21(1):169-72.
6
Influence of ramipril on release of norepinephrine during sympathetic nerve stimulation in isolated rabbit hearts.雷米普利对离体兔心交感神经刺激期间去甲肾上腺素释放的影响。
Zhongguo Yao Li Xue Bao. 1988 Jul;9(4):320-2.
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Metabolism of norepinephrine released by phenoxybenzamine in isolated guinea-pig atria.苯氧苄胺在离体豚鼠心房中释放的去甲肾上腺素的代谢
J Pharmacol Exp Ther. 1972 Feb;180(2):286-301.
8
The inhibition of monoamine uptake into rat brain synaptosomess by selected bicyclo-octanes and an analogous bicyclo-octene.特定双环辛烷及类似双环辛烯对大鼠脑突触体中单胺摄取的抑制作用
Biochem Pharmacol. 1978;27(24):2907-9. doi: 10.1016/0006-2952(78)90207-1.
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Reserpine-induced release of norepinephrine from isolated spontaneously beating guinea-pig atria.利血平诱导去甲肾上腺素从离体自发搏动的豚鼠心房释放。
J Pharmacol Exp Ther. 1971 Jan;176(1):149-59.
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Effects of pre- and post-treatment with EXP 561 on the amine-depleting effects of p-chloroamphetamine and 6-hydroxydopamine in rats.EXP 561 预处理和后处理对大鼠中对氯苯丙胺和 6-羟基多巴胺的胺耗竭作用的影响。
Res Commun Chem Pathol Pharmacol. 1978 Sep;21(3):457-65.

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The clinical pharmacology of intranasal l-methamphetamine.左旋甲基苯丙胺鼻腔给药的临床药理学
BMC Clin Pharmacol. 2008 Jul 21;8:4. doi: 10.1186/1472-6904-8-4.